4-amino-N-(1H-benzimidazol-2-yl)benzamide

Base Information

Chemical Name:4-amino-N-(1H-benzimidazol-2-yl)benzamide
CAS No.:36855-69-3
Molecular Formula:C₁₄H₁₂N₄O
Molecular Weight:252.275
Hs Code.:
DSSTox Substance ID:DTXSID801280419
Nikkaji Number:J2.380.422K

Synonyms:4-amino-N-(1H-benzimidazol-2-yl)benzamide;SCHEMBL16562173;DTXSID801280419;AKOS000321766;36855-69-3;4-Amino-N-1H-benzimidazol-2-ylbenzamide;N-(1H-Benzoimidazole-2-yl)-4-aminobenzamide;AT-057/43469664

Suppliers and Price of 4-amino-N-(1H-benzimidazol-2-yl)benzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-amino-N-(1H-benzimidazol-2-yl)benzamide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:252.10111102
Heavy Atom Count:19
Complexity:327

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)NC(=O)C3=CC=C(C=C3)N

Technology Process of 4-amino-N-(1H-benzimidazol-2-yl)benzamide

There total 6 articles about 4-amino-N-(1H-benzimidazol-2-yl)benzamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 79.4%

: 36855-68-2
4-nitro-N-(1H-benzimidazol-2-yl)benzamide

: 36855-69-3
4-amino-N-(1H-benzimidazol-2-yl)benzamide

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol;
DOI:10.3987/COM-06-10844

Reference yield: 74.32%

: 934-32-7
1H-benzimidazol-2-amine

: 66493-39-8
4-(N-tert-butoxycarbonyl)aminobenzoic acid

: 36855-69-3
4-amino-N-(1H-benzimidazol-2-yl)benzamide

Guidance literature:: 1H-benzimidazol-2-amine; 4-(N-tert-butoxycarbonyl)aminobenzoic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 24h;

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.5h;